Composition comprising photochemical acid progenitor and specific squarylium dye

ABSTRACT

Photochemical acid progenitors in combination with dihydroperimidine squarylium dyes have been found to be particularly effective at generating acid upon irradiation with new-infrared radiation. It has been found that dihydroperimidine squarylium dyes that are particularly useful in this invention have an oxidation potential greater than about 0.5 V relative to SCE as measured in dichloromethane.

FIELD OF THE INVENTION

This invention relates to compositions for the photogeneration of acid.This invention also relates to processes for the photogeneration ofacid.

BACKGROUND

Many processes are known using a medium which, when irradiated withelectromagnetic radiation, generates an acid This acid is then used tocause a change in the properties of the medium, so that exposed andunexposed portions of the medium differ in their properties. Forexample, many photoresist compositions arc of this type; the acidproduced upon exposure to (typically) ultraviolet radiation changes thesolubility of the photoresist composition in the solution used todevelop the photoresist In most conventional acid-generating photoresistprocesses, the sensitivity of the medium an the exposing radiation isnot of major concern. Exposure is normally effected using powerfulultraviolet sources. In addition, long exposures times can usually betolerated.

Today, many imaging processes are being developed using near Infraredradiation from semiconductor diode lasers. Semiconductor diode lasershave the advantage of being much less expensive than ultraviolet lasers.They are also well adapted for the production of high resolution imagesand for digital imaging processes (i.e., for producing hard copies ofimages stored on computers in digital farm). The cost per unit Intensityis less for an infrared producing high-resolution addressable sourcethan for a comparable ultraviolet radiation producing source. Theimaging speed of such infrared radiation using processes is presentlylimited by the sensitivity of the medium, and accordingly, there is aneed to develop infrared sensitive imaging media with improvedsensitivity.

Oftentimes, the sensitivity of photosensitive compositions can beincreased if the photosensitive molecule catalyzes a secondary reactionwhich is not radiation-dependent, and if the photosensitive moleculealso effects conversion of several molecules for each quantum ofelectromagnetic energy absorbed. For example, photoresist systems are(mown in which the primary photochemical reaction produces an acid, andthis acid is employed to eliminate acid-labile groups in a secondary,radiation-independent reaction. See, for example, U.S. Pat. Nos.3,923,514 and 3,915,706. Also, U.S. Pat. No. 5,094,371 discloses aradiation-sensitive mixture which contains a water-insoluble bindercomprising a mixture of phenolic and novolak polymers soluble ordispersible in aqueous alkali, and an organic compound whose solubilityto alkaline developer is increased by acid, and which also contains atleast one acid-cleavable group, and in addition a further group whichproduces a strong acid upon exposure to radiation. A secondary acidgenerator (when used) “ampiffies” the acid produced by an iodonium askor other super-acid precursor, resulting in several molecules of acidbeing produced for each molecule of superacid originally produced bydecomposition of the iodonium still. However, despite the increase insensitivity achieved by such acid amplification, the contrast, and hencethe quality of the resultant image is still governed by the additionalphotochemical acid generation step. Accordingly, it is desirable tosecure as high a quantum yield as possible during the photochemical acidgeneration step.

U.S. Pat. No. 5,286,604 discloses the use of a squarylium dye as a nearinfrared (NIR) light-to-heat converter for the thermal cleavage oftetrahydropyran groups from derivatized polyacrylate and methacrylatepolymers for application in color proofing materials. However, thesensitivity of this system is quite low, i.e., 300-600 mJ/cm². There isno disclosure of a squarylium dye used as a spectral sensitize forlatent Bronsted acid generators.

U.S. Pat No. 5,225,316 discloses the use of various classes of dyesincluding, but not limited to, aryl nitrones, xanthenes, anthraquinones,substituted-diaryl and triaryl methanes, methines, merocyanines, andpolymethines, thiazoles, substituted- and unsubstituted-polycyclicaromatic hydrocarbons, and pyrylium dyes in combination with iodoniumsalts for the photochemical imagewise generation of acid to cleavetetrahydropyran groups from derivatized polyacrylate and methacrylatepolymers for application in no-process printing plates. However nomention was made specifically of squarylium dyes.

European Patent Publ. No. 568,993 discloses combinations of squaryliumdyes and latent Bronsted acid generators (iodonium salts,trichloromethyl-substituted triazines, etc.) for the generation of acidby exposure to visible and NIR light The acid that is generatedcatalyzes various imaging mechanisms including thermal crosslinking andthermal deprotection of hydrolyzable groups from polymers. Severalexamples describe the thermal crosslinking of phenolic resins andmelamine formaldehyde resins catalyzed by acid photogenerated bycombinations of squarylium dyes and tris(trichloromethyl-s-triazine).None of the squarylium dyes disclosed contain a 2,3-dihydroperimidineterminal group.

U.S. Pat. No. 5,340,699 discloses the use of NIR squarylium dyes incombination with latent Bronsted acid generators such asdiphenyliodonium salts or trichloromethyl-containing molecules togenerate a strong Brousted acid which is used to catalyze the thermalcrosslinking of a combination of novolak resin and resole resin.

U.S. Pat. No. 5,401,607 discloses an acid-generating medium comprisingan iodonium salt and a squarylium dye in which the squarylium dyeabsorbs in the range of 700-1200 nm. The squarylium dye preferably hasan oxidation potential in methylene chloride of not greater than 500 mVrelative to the saturated calomel electrode (SCE). This patent teachesthat dyes having oxidation potentials greater than about 500 mV werefound not an be good acid generators.

U.S. Pat No. 4,554,238 discloses the use of sensitizing dyes in therange 300-900 nm as electron donor sensitizers of nitrobenzyl-blockedsurfactants an release the Bronsted acid form of the surfactant Thepatent states that spectral sensitizing compounds suitable for theinvention include those disclosed in the art as being suitable for thespectral sensitization of photolyzable organic halogen compounds(including trichloromethyl-substituted triazines), and sulfonium andiodonium salts. NIR squarylium dyes are disclosed, but there is noteaching that squarylium dyes can sensitize latent Brousted acidgenerators.

K. A. Bello, S. N. Corns and J. Griffiths, J. Chem. Soc, Chem. Commun.,452-454,1993 describes the condensation of 2,3-dihydroperimidines withsquaric acid to give squarylium dyes having absorption maxima near 800nm.

SUMMARY OF THE INVENTION

In one embodiment, the present invention provides an acid-generatingmedium comprising:

(a) a photochemical acid progenitor; and

(b) a squarylium dye having a nucleus of the general formula:

wherein:

R′ to R⁴ are independently selected from hydrogen, alkyl, cycloalkyl,aralkyl, carboalkoxyalkyl and carboaryloxyalkyl groups;

X represents <CR⁵R⁶, <POR⁷, or <BOR⁷

wherein:

R⁵ and R⁶ are independently selected from hydrogen, alkyl, cycloalkyl,aryl, and aralkyl groups;

or R¹ and R⁵, and/or R² and R⁶, and/or R³ and R⁵, and/or R⁴ and R⁶,and/or R⁵ and R⁵ represent the necessary atoms to complete a 5-, 6- or7-membered ring; and

R⁷ represents an alkyl group.

It will be readily appreciated that the dyes of formula (I) may berepresented by a number of different resonance structures, reflectingthe many different ways in which the delocalized π-electron system maybe visualized and notated In formula (I) and elsewhere in thisspecification, the moiety:

represents the aromatic dication derived from cyclobutadiene. Thisparticular notation is chosen for convenience, and allows both the endgroups and the central portion of the dye molecule to be depicted infull aromatized form. It must be emphasized, however, that formula (I)is to be interpreted as including all the possible resonance forms, suchas:

and the like.

In another embodiment, this invention provides an acid generating mediumcomprising:

(a) a photochemical acid progenitor selected from the group consistingof diaryliodonium salts, aryldiazonium salts, and1.3.5-tris(trichloromethyl)-s-triazines; and

(b) a squarylium dye having an oxidation potential in dichloromethanegreater than or equal to 0.5 V and less than or equal to 0.8 V relativeto a standard calomel electrode.

This invention also provides a process for generating acid, comprisingthe steps of:

(a) providing a mixture of a photochemical acid progenitor and asquarylium dye of the formula (I) disclosed earlier herein; and

(b) irradiating the mixture with radiation from a light source,preferably a laser emitting in the near infrared region (700 to 1200 nm)of the spectrum.

It is generally accepted in the field of the present invention to allowsubstantial substitution on the core dye structure of the presentinvention. Some types of substitution, especially that which improvessolubility in a selected solvent, is particularly desirable. Where theterm “group” or “central nucleus” is used in describing an aspect of thepresent invention, that term implies that any type of substitution isacceptable, as long as the basic structure is maintained. For example,“alkyl group” would include not only standard hydrocarbon alkyls such asmethyl, ethyl, cyclohexyl, isooctyl, undecyl, etc., but would alsoinclude substituted-alkyl such as hydroxymethyl, omega-cyanopropyl,1.2.3-trichlorohexyl, 1-carboxy-isooctyl, phenyldecyl, and the like. Theterm “alkyl” or “alkyl moiety” indicates that there s no substitution onthat defined component.

Other aspects, advantages, and benefits of the present invention areapparent from the detailed description, examples, and claims.

DETAILED DESCRIPTION OF THE INVENTION

Squarylium dyes of the present invention have a nucleus of the generalformula:

wherein:

R¹ to R⁴ are independently selected from hydrogen, alkyl, cycloalkyl,aralkyl, carboalkoxyalkyl and carboary-loyalkyl groups;

X represents <CR⁵R⁵, <POR⁷, or <BOR⁷

wherein:

R⁵ and R⁶ are independently selected from hydrogen, alkyl, cycloalkyl,aryl, and aralkyl groups;

or R¹ and R³, and/or R² and R⁶and/or R³ and R³, and/or R⁴ and R⁵, and/orR³ and R⁵ represent the necessary atoms to complete a 5-, 6-or7-membered ring; and

R⁷ represents an alkyl group.

Preferably, R¹ to R⁴ are independently selected from hydrogen; asubstituted or unsubstituted alkyl or cycloalkyl group having from 1 to20 carbon atoms; an aralkyl group having from 6 to 20 carbon atoms suchas benzyl or p-dodecylbenzyl; a carboalkoxyalkyl group with the alkoxygroup having from 1 to 20 carbon atoms such as carboethoxymethyl orcarbooctyloxymethyl; and a carboaryloxyalkyl group with the aryloxygroup having from 5-20 carbon atoms such ascarbo(p-dodecylphenol)methyl. Dyes in which one or more of R¹ to R⁴ areother than hydrogen show enhanced solubility in organic solvents such asmethylethylketone and 1-methoxy-2-propanol.

Preferably, R⁵ and R⁶ are independently selected from hydrogen; an alkylor cycloalkyl group having from 1 to 20 carbon atoms; and a substitutedor unsubstituted aryl group having from 5 to 20 carbon atoms. Examplesof preferred groups from which R⁵ and R⁶ may be selected include —CH₂OH,—CH₂OR⁸, —CH₂OCH₂CO₂R⁸, —CH₂OSO₂R⁹, and —CH₂OSi(R⁹)₃, wherein R⁸ isindependently an alkyl, alkaryl, aralkyl or aryl group and R⁹ isindependently an alkyl or alkaryl group. In addition, R⁵ and R⁶ takentogether may form a 5- to 7-membered nucleus (e.g., heterocyclic,carbocyclic, etc.).

R¹ and R⁵, and/or R² and R⁶, and/or R³ and R⁵, and/or R⁴ and R⁶, and/orR⁵ and R⁶ taken together may represent the necessary atoms to complete a5-, 6- or 7-membered ring. One example of the above situation would bewhere R¹ and R², and/or R³ and R³ are taken together to form a lactamgroup; R⁶ is an alkyl or aryl group; and R³ and R⁴ are hydrogen.

Preferably, R⁷ represents an alkyl group having from 1 to 20 carbonatoms.

Preferably, R⁸ is independently selected from an alkyl, alkaryl, aralkylor aryl group having from 1 to 20 carbon atoms.

Preferably, R⁹ is independently an alkyl or alkaryl group having from1to 20 carbon atoms.

Squarylium dyes used in the present invention can be made according toprocedures disclosed later herein, as well as those disclosed in U.S.Pat. Nos. 5,360,694 and 5,380,635.

Conventional photochemical acid progenitors (hereinafter known as acidprogenitors) well known in the art can be used in the present invention.Non-limiting examples include s-triazine compounds substituted with atleast one trihalomethyl group such as2,4,6-tris(trichloromethyl)-s-triazine,2-(4-methoxyphenyl)-4,6-bis-(trichloromethyl)-s-triazine,2-(4-methoxy-1-naphthalenyl)-4,6-bis(trichloromethyl)-s-triazine and thelike, iron-arena complexes such as(η⁶-isopropylbenzene)(η³-cyclopentadienyl)iron (II) hexafluorophosphate,(η⁶-xylenes) (η³-cyclopentadienyl) iron (II) hexaflucroantimonate andthe like, and onium salts such as diaryliodonium salts, triaysulfoniumsalts, triarylselenonium salts, dialkylphenacylsulfonium salts,dialkyl-4-hydroxyphenylsulfonium salts, aryldiazonium salts, nitrobenzylesters such as p -toluenesulfonic acid ester of p-nitrobenzyl alcoholand the like, sulfonic acid esters such asα-hydroxymethylbenzoinsulfonic acid ester and the like.

The imaging medium of the present invention desirably comprises abinder, preferably a polymeric binder, which serves to bind the infrareddye and the photochemical acid progenitor into a coherent layer whichcan be handled easily.

Non-limiting examples of binders include polymers and copolymers ofacrylic acid or esters thereof, methacrylic acid or ester thereof,(anhydrous) maleic acid or esters thereof, acrylonitrile, styrene,α-alkylstyrene, α-acetoxystyrene, hydroxystyrene, α-alkylhydroxystyrene,α-acetoxyhydroxystyrene, or the substituted compounds obtained byprotecting the hydroxy groups of the above compounds with a protectinggroup easily hydrolyzable by acid treatment (for example, trialkylsilylgroup, tetrahydropyranyl group, t-butoxycarbonyl group and the like), orcyclic analogues thereof, vinyl acetate, vinyl chloride, vinylidenechloride, butadiene, crotonic acid, itaconic acid, N-substitutedmaleimide, vinyl benzoate, or copolymer of the above esters,polyethylene oxide, polyvinyl pyrrolidone, polyamide, polyurethane,polyethylene terephthalate, acetyl cellulose, methyl cellulose, ethylcellulose, polyvinyl butyral, chlorinated polyolefin, polyalkylene,polyaldehyde, polycarbonate, epoxy resin, cresol novolak resin, resoleresin, melamine resin, alkyd resin, modified polyvinyl alcohol, or blockor graft copolymer or modified polymer by combination of them and thelike. For applications such as positive acting printing plates, resistsand proofs, binders which do not require a post exposure heating stepbefore development will be preferred. Such binders include, for example,the homo- and copolymers of tetrahydropyranyl (meth)acrylate.

For improving the plasma-resistance upon development, a substituentcontaining silicone may be introduced in the binder before or afterexposure to light.

Preferably, the proportion of the squarylium dye of formula (I) is 0.01to 0.6 puts by weight (referred to as “part” hereinafter) relative toone part of acid progenitor, and preferably, the amount of the binder is2 to 100 parts, and more preferably, 5 to 50 parts, relative to one partof the acid progenitor.

Though not wishing to be limited or restricted by my theory or mechanismfor acid generation in the present invention, the process of acidformation from the combination of near infrared dyes of the presentinvention with acid progenitors may take place by one of severalmechanisms. Efficient energy transfer from an excited state of a donorto a ground state receptor requires that the excited state energy of thedonor is higher than the excited state energy of the receptor, as iswell known in the art. Therefore, energy transfer from the irradiatedexcited state of the near infrared dye to the acid progenitor isunlikely due to the high singlet and triplet energies of the acidprogenitors and the low excited state energies of the near-infrared dyesused in the present invention.

One method of introducing light energy in an imagewise fashion is theuse of short pulses of high intensity laser light to excite the nearinfrared dyes of the present invention. The excited state of theirradiated near infrared dye can undergo radiationless transition backto the ground state of the dye resulting in light-to-hew conversion asis well known in the art. Depending on the fluence of the laser source,several hundreds of degrees centigrade can be achieved during the pulseor dwell time of the laser light. These high temperatures could thenresult In the thermal decomposition of the acid progenitors to produceacid. According to this mechanism, one might expect the sensitivity ofthe media of the present invention to be independent of the structure ofthe near infrared dyes used in the present invention since all of thedyes used in the present invention are capable of light-to-heatconversion. However, the sensitivities of the media used In the presentinvention are dependent on the dye structure. Although the light-to-heatconversion mechanism may still contribute to the generation of acid inthe present invention, it does not appear to be the sole or dominantmechanism.

One possibility is that sensitization of acid progenitors bynear-infrared dyes used in the present invention requires electrontransfer from the excited state of the irradiated near-infrared dye tothe acid progenitor. It is well known in the art that the efficiency ofelectron transfer depends strongly on the free energy flange, AGO,associated with photoinduced electron transfer, in this case from theexcited state of the near-infrared dye to the acid progenitor. This freeenergy flange may be expressed by the Rehm-Weller relationship (D. Rehmand A, Weller, Isr. J. Chem, 1970, 8, 259) as follows:

 ΔG⁰=(E _(ox) ^(sens) -E _(red) ^(init) e ₀ ² /ea)-E _(0,0) ^(sens)

where E_(ox) ^(sens) and E_(red) ^(init) are the ground state oxidationpotential of the sensitizing near-infrared dye and reduction potentialof the acid progenitor initiator, respectively, and E_(0,0) ^(sens) isthe excitation energy of the 0,0 band of the sensitizing near-infrareddye. According to the Rehm-Weller relationship, the efficiency ofelectron transfer increases as the oxidation potential of thesensitizing dye becomes less positive and the reduction potential of theacid progenitor initiator becomes less negative. Indeed theeffectiveness of the near-infrared dyes used in the present invention ingenerating acid has been found to correlate with the oxidation potentialof the near-Infrared dye. Accordingly, it is preferred that the dye usedin the present invention have an oxidation potential in dichloromethanenot greater than about 0.8 V, and more preferably, not greater thanabout 0.7 V, relative to a standard calomel electrode when the acidprogenitor is diaryliodonium salts, aryldiazonium salts, or1,3,5-tri(trichloromethyl)-s-triazine. Dyes having oxidation potentialsgreater than about 0.8 V have been found not to be good sensitizers ofacid progenitors, presumably because the high oxidation potential of thedye readers the free energy change ΔG⁰ for electron transfer between theexcited state of the near-infrared dye and the acid progenitorunfavorable. The preferred oxidation potential of near infrared dyesused in the present invention may vary, of course, for sensitization ofacid progenitors of lower or higher reduction potential.

However, as the oxidation potential of the near infrared sensitizing dyebecomes less positive and the reduction potential of the acid progenitorinitiator becomes less negative, ground state electron transfer from thenear infrared dye to the acid progenitor initiator becomes morefavorable. (round state electron transfer from the near infrared dye tothe acid progenitor initiator can also lead to the formation of acid,which in turn can lead to instability of the imaging composition andshelf life problems which render the imaging composition useless.Therefore, as the oxidation potential of the sensitizing near-infrareddyes of the present invention becomes too low, shelf life problems mayoccur. Indeed the stability of the imaging compositions of the presentinvention have been found to correlate with the oxidation potential ofthe near-infrared dye. Accordingly, it is preferred that the dye used Inthe present invention has an oxidation potential in dichloromethanegreater than about 0.55 V, and more preferably, greater than about 0.60v, relative to a standard calomel electrode, if the acid progenitor is adiaryliodonium salt, aryldiazonium salt, or 1,3,5-tris(trichloromethyl)-s-triazine. The instability observed under acceleratedaging conditions (3 days at 60° C.) indicates that imaging mediacontaining near infrared dyes used in this invention having oxidationpotentials less than about 0.60 V would have limited utility when usedwith acid progenitors such as diaryliodonium salts, aryldiazonium sales,or 1,3,5-tris(trichloromethyl)-2,4,6-triazine.

Imaging compositions containing the near infrared dyes used in thepresent Invention having oxidation potentials in the range of about 0.5V to about 0.7 V have been found to have sufficient sensitivities to beuseful in practice when the acid progenitor is diaryliodonium salts,aryldiazonium salts, or 1,3,5-tris(trichloromethyl)-s-triazine. Priorart near infrared dyes as disclosed in U.S. Pat No. 5,401,607 were foundnot to be useful for sensitizing acid progenitors such as diaryliodoniumsalts when their oxidation potentials in dichloromethane were greaterthan about 0.5 V versus the standard calomel electrode.

A beneficial property of the near infrared dihydroperimidine squaryliumdyes used in the present invention is their ability to achieve a widerange of oxidation potentials in the range of about 0.5 V to about 0.9 Vby manipulation of the dihydroperimidine end group substituents. In thismanner, the oxidation properties of the dye can be manipulated to givethe best properties of sensitivity and shelf life in conjunction withthe particular acid progenitor and imaging construction chosen.

Imaging compositions containing infrared dyes used in the presentinvention may be used to initiate any of the acid-dependent reactionsinitiated by prior art acid-generating reactions which produce an acidof comparable strength. Preferred acid-dependent reactions relate tochemical amplification resist compositions of the negative and positivetype which can be characterized by high sensitivity to visible and nearinfrared regions of the electromagnetic radiation spectrum For example,the present process may be used to trigger an acid-catalyzedpolymerization reaction, an acid-catalyzed crosslinking reaction, anacid-catalyzed depolymerization reaction, so acid-catalyzedde-protection reaction, or an acid-catalyzed destruction of dissolutioninhibiting agent.

For example, a negative type resist using a thermal acid-catalyzedcrosslinking reaction represented by the acid-catalyzed crosslinking ofphenolic resins by a crosslinking agent, is known (U.S. Pat No.5,368,783). Such resists may require a heat treating step following thelight Irradiation. In this case it is preferred that the developmenttemperature is less than the decomposition temperature of the acidgenerating initiator.

Compounds which may be used as crosslinking agents include aminocompounds having as functional groups at least two alkoxymethyl groups,methylol groups, or acetoxymethyl groups and the like. Examples includemelamine derivatives (e.g., hexamethoxymethylated melamine, availablefrom Mitsui-Cyanamid, Ltd. as CYMEL® 300 series (1) and the like);benzoguanamine derivatives (e.g., methylethyl mixed alkylatedbenzoguanamine resin, available from Mitsui-Cyanamid, Ltd. as CYMEL(r)1100 series (2)) and the like); and glycoluril derivatives (e.g.,tetramethylolglycoluril, available from Mitsui-Cyanamid, Ltd. as CYMER®1100 series (3) and the like). Also included are di-substituted aromaticcompounds having functional groups such as alkoxymethyl groups, methylolgroups, acetoxymethyl groups and the like. Examples of such compoundsinclude 1,3,5-trihydroxymethylbenzene, 1,3,5-triacetoxymethylbenezene,1,2,4,5-tetraacetoxymethylbenzene and the like. These crosslinkingagents can be synthesized according to the method described in PolymMater. Sol. Eng., 64, 241 (1991).

The amount of the crosslinking agent is preferably 0.1 to 100 parts,more preferably 0.2 to 50 parts, relative to one part of thephotochemical acid generator.

Positive type resists based on acid-catalyzed de-protection reactionsare known. For example, the de-protection of tetrahydropyran groups fromderivatized polyacrylate and methacrylate polymers in which the exposedmaterial becomes soluble in developer is disclosed in U.S. Pat. No.5,102,771.

Positive type resists based on the acid-catalyzed destruction of adissolution inhibiting agent in which the exposed material becomessoluble in developer are disclosed in European Patent Publ. No. 424,124and U.S. Pat No. 5,085,972. Such positive type resists consist of, forexample, a novolak redo, a dissolution inhibiting agent such as thebis-tetrahydrofuranyl ether of bisphenol A, an acid progenitor such as adiaryliodonium salt, and a sensitizing dye for the acid progenitor.

Further, solvent (such as methylethylketone, 1-methoxy-2-propanol, ethylcellosolve and the like), plasticizer (such as dioctyl phthalate and thelike), dark reaction inhibitor, colorant composed of organic orinorganic dye or pigment and the like may be contained therein dependingupon the use of the chemically amplifying resist.

A composition of the present invention is prepared, for example, bymixing the dye of formula (I), an acid progenitor, a binder and, ifnecessary, a crosslinking agent or dissolution inhibitor or the like.This composition may be mated by any method (mown in the art (e.g.,knife coating, bar mating, curtain coating, etc.) on a substrate. Thenature of the substrate is not critical and includes, for example,paper, plastic, glass, metal plates, etc. For example, a photosensitivematerial having high sensitivity to near Infrared radiation can beprepared by coating a solution of the composition of the presentinvention dissolved in a solvent (such as methylethylketone and thelike) on an aluminum plate having a treated surface, a silicon wafer, aglass plate, or a plastic film and the like and drying.

In the practice of the present Invention, light sources from the visibleto near infrared are used to deliver an electromagnetic radiationpattern which can be absorbed by the dye of formula (I) in the imaginglayers. Suitable light sources include mercury lamps, carbon are lams,xenon lamps, metal halide lamps, tungsten lamps, halogen lamps, flashlamps, light-emitting diodes, laser rays, semiconductor diode lasers,Ti-Sapphire lasers and the like.

It is advantageous to employ light sources which are relatively richerin near infrared wavelengths. Preferred non-laser light sources includehigh power (250 W to 10 kW) tungsten lamps and xenon lamps. When a laseris used it is preferred that it emit in the and or near infrared regionof the electromagnetic spectrum, especially from about 700 to 1200 am.Suitable laser sources In this region include Nd:YAG, Nd:YLF andsemi-conductor lasers. The preferred lasers for use in this inventioninclude high power single mode laser diodes, fiber-coupled laser diodearrays, and laser diode bars producing 0.1 to 12 W in the near infraredregion of the electromagnetic spectrum.

The entire construction may be exposed at once, or by scanning, or witha pulsed source, or at successive times in arbitrary areas. Simultaneousmultiple exposure devices may be used, including those in which thelight energy is distributed using optical fibers, deformable micromirrorarrays, light valves, and the like. Preferably, a solid state infraredlaser or laser diode array is used. Sources of relatively low intensityare also useful, provided they are focused onto a relatively small area.If a non-laser light source is used, the entire construction may beexposed at once through an image mask, such as a graphic arts film maskor a chrome glass mask.

Exposure may be directed at the surface of the imaging layer containingthe Imaging materials of this invention, or through a transparentsubstrate beneath such an imaging layer. Exposure energies will dependon the type of sensitizer of compound (I), the type of photochemicalacid generator, and the type of materials used in creating a negative orpositive Image. The rate of scanning during the exposure may also play arole. Exposure energies will be chosen so as to provide a degree of cureor reaction to be useful for the particular application. Laser exposuredwell times are preferably about 0.05 to 50 microseconds and laserfluences are preferably about 0.001 to 1 J/cm². Non-laser exposure dwelltimes are preferably about 5 seconds to about 10 minutes and financesare preferably about 0.01 to 1 J/cm².

The following non-limiting examples further illustrate the presentinvention.

EXAMPLES

Instrumentation

All cyclic voltammograms were measured in dichloromethane containing0.2M tetrabutylammonium tetrafluoroborate and 12 mg dye using a BAS100B/W Electrochemical Analyzer (Bioanalytical Systems, Inc., WestLafayette. Ind.). Where the oxidation is reversible, E_(½), representsthe average of the voltage values for E_(a) the anodic peak current, andE_(c), the cathodic peak current, observed in the cyclic voltammogram.The CV was run at 50 millivolts per second unless stated otherwise. Theworking electrode consisted of a 1 millimeter platinum wire imbedded inglass to give a surface area of 0.78 mm². The counter electrode was aplatinum wire. The reference electrode was SCE. The cyclic voltammogramswere corrected for the background signal for dichloromethane andtetrabutylammonium tetrafluoroborate solution.

Near Infrared/visible absorption spectra were measured using a ShimadzuMPC-3100 spectrophotometer (Shimadzu, Inc., Columbia, Md.). Absorptionspectra of coatings on opaque substrates were made using the integratingsphere attachment for the Shimadzu spectrophotometer.

Laser Diode Exposure Assembly

Coated samples were taped to an external drum scanning configuration andscanned from the coating side using a focused laser spot from acollimated/circularized laser diode (SDI, Inc., San Jose, Calif., Model5422-G1, 811 nm). The focused spot size was 8μ (full width at e⁻² level)and the power at the media was 110 mW The cross-scan translation ratewas 4.5μ/drum rotation. The circumference of the drum was 84.8centimeters. Image data was transferred from a mass-memcry system andsupplied to the power supply which performed the image-wise modulationof the laser diode.

Materials

All materials for which preparation procedures are no given wereobtained commercially, many from Aldrich Chemical Co., Milwaukee, Wis.Synthesized compounds were characterized such as by their ¹H and ¹³NMR,and IR spectra. The preparation of poly (tetrahydropyranylmethacrylate)is described in U.S. Pat. No. 5,102,771. Dyes 1a and 1g were prepared asdescribed in U.S. Pat. 5,380,635. Dye 1 h was prepared as described inWO Patent Application 92/09661. Dye 1i was prepared according to themethod described in Kuramoto et al., Dyes and Figments, 1989, 11, 21.

Preparation of 2,2-Bis(hydroxymethyl)-2,3-dihydro-1H-perimidine.

A mixture of 87.49 g (0.553 mol) of 1,8-diaminonaphthalene, 54.05 g(0.300 mol) of 1,3-dihydroxyacetone dimer, 38 mg of p-toluenesulfonicacid monohydrate, and 500 mL of absolute ethanol was refluxed for 33 hr.To the still ho solution was added 1 mL of concentrated ammoniumhydroxide in 9 ml, of water, and the mixture was poured into a beaker tocool and crystallize. After standing overnight, the product was filteredoff and air dried to yield 97.806 g of the bis(hydroxymethyl)dihydroperimidine;

Preparation of Intermediate Dye A

A mixture of 28.00 g (0.1216 mol) of 2,2-bis(hydroxymethyl)-2,3-dihydro-1H-perimidine, 6.935 g (0.0608 mol) ofaquatic acid, and 200 ml. of 1-propanol was heated at reflux withstirring for 1 hr. Then 25 ml. of the solvent was distilled out, and themixture cooled to room temperature. After 3 hr, a solid was filtered offand dried, yielding 29.445 g of Inter mediate Dye A:

Intermediate Dye A was found to have a λ_(max) of 808 nm intetrahydrofuran.

Preparation Dye 1b

A mixture of 14.19 g (0.03851 mol) of 2,2-dibenzyl-2,3-dihydroperimidine(prepared by the condensation of 1,3-diphenylacetone with1,8-diaminonaphthalene according to the general procedure found in U.S.Pat. No. 5,380,635), 2.196 g (0.01926 mol) of aquatic acid, and 50 ml.of n-octanol were heated with stirring under a Dean-Stark trap at apressure of 40 torr at reflux for 48 min with water separation. Aftercooling an room temperature, the crude dye was filtered off, washed withheptane and with petroleum ether, and air dried to obtain 13.60 g. Thiswas further purified by chromatography on a silica gel column gradienteluted with methylene chloride/heptane mixtures, collecting the greencolored band. The dye had λ_(max) 824 nm (MeOH).

Preparation Dye 1c

A mixture of 0.250 g (0.000464 mol) Intermediate Dye A, 0.142 g (0.00209mol) of imidazole, and 0315 g (0.00209 mol) of (t-butyl-dimethylsilylchloride was shred in 10 ml of dimethylformamide at room temperature for18 hr. The mixture was poured into 240 ml of water, and the crudeproduct was filtered off after 3 hr. Chromatography on a 20×190 cmsilica gel column eluting with 25% ethyl acetate in heptane yielded0.157 g of Dye 1 c, as the initial band λ_(max)=800 nm (ethyl acetate).

Preparation of Dye 1d

(a) 1,3-dihydroperimidine derivative I

A mixture of 2,2-bis(hydroxymethyl)-2,3-dihydro-1H-perimidine (4.14 g,18.0 mmol), benzene (45 mL), 50% aqueous sodium hydroxide (37.5 mL),tetrabutylammonium hydrogen sulfate (1.0 g, 2.94 mmol), and t-butylbromoacetate (5.85 mL, 39.6 mmol) was vigorously stirred at roomtemperature for 18 hours using a mechanical stirrer. The reactionmixture was diluted with water (150 mL) and then extracted twice withchloroform (150 mL each). The chloroform extracts were combined andwashed with brine (100 mL). The chloroform layer was dried usinganhydrous magnesium sulfate, filtered, and then concentrated to give atan solid. The solid was recrystallized with methanol to yield 3.90 g of1,3-dihydroperimidine derivative I as tan crystals; m.p. 152°-154° C.;¹H NMR (500 Mz; CDCl₃): δ 1.46 (s, 18H); 3.70 (s, 4H); 4.01 (s, 5H);5.20 (s, 2H); 6.51 (δ, 2H, J=7.3 Hz); 7.12 (δ, 2H, J=8.1 Hz); 7.21 (t,2H, J=7.8 Hz); ¹³C{¹H} NMR (125 Mz; CDCl₃): δ 28.00, 67.09, 69.43,72.53, 81.75, 105.88, 112.33, 116.87, 126.92, 134.34, 138.74, 169.56.

(b) Dye 1d. A mixture of the 1,3-dihydroperimidine derivative from part(a) (0.687 g, 1.5 mmol), squaric acid (0.086 g, 0.75 mmol), n-butanol (9mL) and toluene (9 mL) was heated at reflux for 4 hours. The reactionmixture was allowed to cool and stand at room temperature overnight. Thereaction mixture was filtered and the residue was washed with ethanol.The residual solid was dried under reduced pressure to give 0.420 g ofDye 1d as a dark blue solid, λ_(max)800 nm (acetone).

Preparation Dye 1e

A mixture of 15.57 g (0.1157 mol, 16.2 mL) of hexanoyl chloride in 40 mLof THF was added dropwise over 4 hr to a stirred mixture of 15.581 g(0.02893 mol) of Intermediate Dye A, 14.138 g (0.1157 mol) of4-dimethylaminopyridine, and 600 mL of THF. After 18 hr at roomtemperature, the mixture was filtered to remove 4-dimethylaminopyridinehydrochloride, the salt washed with a little THF, and the combinedfiltrate evaporated to dryness. The resulting solid was stirred for 45min in 200 mL of heptane, then filtered, and stirred in 200 mL ofmethanol for 50 min. After filtration and drying, 17.018 g wereobtained. This material was recrystallized from ethyl acetate to yield15.260 g of Dye 1e. λ_(max)805 nm (THF), ε=1.63×10⁵.

Preparation Dye 1f

A mixture of 0.828 g (0.00389 mol) of octanesulfonyl chloride in 5 ml oftetrahydrofuran was added over 1 hr to a stirred mixture of 0.524(0.000973 mol) of Intermediate Dye A and 0.475 g (0.00389 mol) of4-dimethylaminopyridine in 16 ml of tetrahydrofuran. After 20 hr, themixture was filtered and the filtrate evaporated to dryness. Theresulting solid was stirred with heptane, filtered, stirred withmethanol, filtered, and chromatographed on a 20×190 cm silica gel columngradient eluted with ethyl acetate in heptane to give 0.360 g of Dye 1f,as the initial band. λ_(max)=804 nm (ethyl acetate).

TTT is 2,4,6-tris(trichloromethyl)-1,3,5-triazine and was preparedaccording to the procedure of K. Wakabayashi, M. Tsunoda, and T. Suzuki,Bull. Chem. Soc. Japan, 1969, 42, 2924.

Ditolyliodonium hexafluorophosphate was prepared according to the methodof U.S. Pat. No. 3,981,897.

(η⁶-Xylenes) (η⁵-cyclopentadienyl) iron (II) hexafluoro-antimonate wasprepared according to the procedure in U.S. Pat. No. 5,059,701.

Dissolution inhibitor 1 (the bis-tetrahydropyranyl ether of bisphenol A)was prepared according to the procedure in European Patent Publ. No.424,124.

Preparation of 2-methoxy-4-phenylaminobenzenediazoniumhexafluorophosphate.

A mixture of 12 grams (37.1 mmol, 1.0 eq) of 2-methoxy-4-(phenylamino)benzenediazonium hydrogen sulfate (TCI America, Portland,Org.) in 600 mL of water was heated to 35°-40° C. and then filtered. Tothe filtrate was added a solution of 9.6 grams (52.0 mmol, 1.4 eq) ofpotassium hexafluorophosphate in 220 mL of water and a precipitateformed immediately. The mixture was stirred for 2 hours and collected byfiltration, washed with water and then with approximately 100 mL ofisopropanol and air dried to give 12.05 grams (87.5% yield) of2-methoxy-4-phenylaminobenzenediazonium hexafluorophosphate.

EXAMPLE 1

A solution consisting of 2 g of 10% Novolak SD-126A (Borden Packaging &Industrial Products, Louisville, Ky.) in methylethylketone, 0.02 g ofCYMEL 303 (American Cyanamid Co., Wayne, N.J.), 0.02 g TTT, and 0.003 gDye 1a was coated with a No. 6 coating rod (R&D Specialties, Webster,N.Y.) onto 200 micron-thick grained and anodized aluminum printing platebase and dried with a heat gun.

A near infrared spectrum (integrating sphere) was taken of a sample ofthis coating when fresh and after 1 and 2 days at 60° C. The results aregiven in Table 1.

A fresh sample of the plate and a sample aged 2 days at 60° C. werescanned with the laser diode exposure assembly. Separate areas of theplate were scanned at a rate of 6, 8, and 10 revolutions per second(508, 678, and 848 centimeters per second, respectively). The scannedplates were heated for 60 seconds at 105° C. and developed with PCXpositive plate developer (3M, St. Paul, Minn.). For the fresh plate, thecoating remained on the plate exposed at all scan rates while thecoating was developed off the plate in the unexposed areas. However, theunexposed coating remained on the plate for the sample aged 2 days at60° C.

TABLE 1 Absorption spectra of plates before and after accelerated agingat 60° C. Dye λ_(max) Abs (λ_(max)) Abs (811 nm) Fresh 800 nm 1.0741.044 1 day, 60° C. 798 nm 0.859 0.835 2 days, 60° C. 808 nm 0.870 0.865

Table 1 shows that the absorption of Dye 1a dropped about 15% onaccelerated aging for 2 days at 60° C. It appears that Dye 1a and TTTgenerate acid thermally; this acid can then catalyze the crosslinking ofthe novolak and melamine resins during the heating step with the resultthat the coating cannot be removed from the unexposed re-ions of theplate. The instability of Dye 1a in the presence of TTT may be due tothe relatively low oxidation potential of Dye 1a (E_(1/2)=0.51 V versusSCE) and the relatively low reduction potential of TTT (peak reductionpotential of approximately −0.83 V versus SCE).

EXAMPLE 2

Example 1 was repeated except that Dye 1e replaced Dye 1a.

A near infrared spectrum was taken of a sample of this coating whenfresh and after 1 and 2 days at 60° C. The results are given in Table 2.

A fresh sample of the plate and a sample aged 2 days at 60° C. wereexposed with the laser diode exposure assembly, heated and developed asin Example 1. Both fresh and aged samples left coating on the plate inthe exposed areas at all scan rates of 6, 8, and 10 revolutions persecond. In addition, there was no coating left in the unexposed areas.There were no signs of degradation of the coating after acceleratedaging for 3 days at 60° C. These results indicate that Dye 1e is morestable than Dye 1a in the presence of TTT. This may be due to the higheroxidation potential of Dye 1e (E_(1/2)=0.68 V vs SCE) relative to Dye 1a(E_(1/2)=0.51 V versus SCE).

TABLE 2 Absorption spectra of plates before and after accelerated agingat 60° C. Dye λ_(max) Abs (λ_(max)) Abs (811 nm) Fresh 803 nm 0.0700.760 1 day, 60° C. 806 nm 0.827 0.813 2 days, 60° C. 805 nm 0.779 0.762

EXAMPLES 3-8 AND COMPARATIVE EXAMPLES 1-2

These examples demonstrate that the shelf life and sensitivity ofcoatings containing novolak resin, melamine formaldehyde resin, TTT andsquarylium dye depend on the oxidation potential of the dye.

Coating formulations consisted of 1.92 g of 17% by weight novolak resinSD-126A in methylethylketone, 0.033 g CYMEL® 303, 0.028 g TTT, and dye.The formulations were coated with a No. 6 coating rod onto 200 micronthick grained and anodized aluminum printing plate base and dried with aheat gun.

Example 3. 0.006 g Dye 1a.

Example 4. 0.006 g Dye 1b.

Example 5. 0.008 g Dye 1c.

Example 6. 0.007 g Dye 1e.

Example 7. 0.009 g Dye 1f.

Example 8. 0.005 g Dye 1g (Dye 1g did not all dissolve in thisformulation.)

Comparative Example 1. 0.005 g Dye 1h.

Comparative Example 2. 0.007 g Dye 1i.

Absorbances at λ_(max) were determined from near infrared spectra(integrating sphere) of a sample of each of Examples 3-8 and ComparativeExamples 1 and 2 when fresh and after aging at 60° C. The results aregiven in Table 3.

Relative sensitivities were determined by exposing a sample of each ofExamples 3-8 and Comparative Examples 1-2 through a Stouffer 21-stepsensitivity wedge (Olson Graphics, St. Paul, Minn.) using a 3M Model 70tungsten light source (3M, St. Paul, Minn.) for 60 seconds (fleshcoatings) or 120 seconds (coatings aged at 60° C.). After exposure, theplates were heated for 30 seconds (fresh coatings) or 60 seconds(coatings aged at 60° C.) at 115° C. The plates were developed using PCXpositive plate developer. Sensitivity is proportional to the number ofsolid steps left on the plate. Solid steps are defined as those steps inwhich all the coating has been left on the plate. An open step isdefined as an area where all the coating has been developed off theplate. Where fogging occurred, the first open step is the step at whichtheir is no perceptible change in background density through step 21.Fogging refers to some residual coating left on the plate in theunexposed areas. The results are given in Table 3.

TABLE 3 λ_(max) Example or ΔE_(p) Absorbance: Comparative E_(1/2) vs.SCE Fresh and after Relative sensitivity of fresh plates and Example(CH₂Cl₂)^(a) aging at 60° C. after aging at 60° C.^(b) 827 nm Example 3ΔE_(p) = 0.074 V Fresh: 0.956 Fresh: Solid 11, Open 15^(a) Dye 1aE_(1/2) = 0.51 V 1 day: 0.708 2 days: 0.667 2 days, 60° C.; Solid 1,Open 4^(d) 5 days: 0.635 5 days, 60° C.; <Solid 1, Some fogging^(d) 834nm Example 4 ΔE_(p) = 0.066 V Fresh: 1.104 Fresh: Solid 5, Open 10^(a)Dye 1b E_(1/2) = 0.54 V 1 day: 0.656 1 day, 60° C.; Solid 4, Open 7^(d)4 days: 0.463 4 days, 60° C.; <Solid 1, No fogging^(d) 823 nm Example 5ΔE_(p) = 0.079 V Fresh: 0.806 Fresh: Solid 8, Open 13^(a) Dye 1^(c)E_(1/2) = 0.61 V 1 day: 0.691 2 days: 0.686 2 days, 60° C.; Solid 1,Open 5^(d) 5 days: 0.675 5 days, 60° C.; Solid 1, Open 5^(d) 818 nmExample 6 ΔE_(p) = 0.077 V Fresh: 0.943 Fresh: Solid 3, Open 8^(a) Dye1e E_(1/2) = 0.68 V 1 day: 0.855 2 days: 0.876 2 days, 60° C.; Solid 3,Open 6^(d) 5 days: 0.834 5 days, 60° C.; Solid 2, Open 6^(d) ΔE_(p) =0.130 V 817 nm Example 7 E_(1/2) = 0.73 V Fresh: 0.797 Fresh: Solid 1,Open 3^(a) Dye 1f (400 mV/sec 1 day: 0.402 sweep rate) 2 days: 0.425 2days, 60° C.; No image, no fogging^(d) 5 days: 0.381 5 days, 60° C.;<Solid 1, Open 4^(d) 813 nm Example 8 ΔE_(p) = 0.094 V Fresh: 0.323Fresh: <Solid 1, open 3^(a) Dye 1g E_(1/2) = 0.89 V 1 day: 0.322 1 day,60° C.: Solid 1, Open 4^(d) 4 days: 0.326 4 days, 60° C.; No image, nofogging^(d) 765 nm Comparative ΔE_(p) = 0.077 V Fresh: 1.24 Fresh: Solid7, open 13^(a) Example 1 E_(1/2) = 0.67 V 1 day: 1.196 1 day, 60° C.:Solid 8, Open 13^(d) Dye 1h 4 days: 1.188 4 days, 60° C.; Solid 8, Open13^(d) 667 nm Comparative ΔE_(p) = 0.077 V Fresh: 0.964 Fresh: Solid 10,open 17^(a) Example 2 E_(1/2) = 0.48 V 1 day: 0.794 1 day, 60° C.: Solid14, Open 21^(d) Dye 1i 4 days: 0.747 4 days, 60° C.; Solid 4, Open11^(d) ^(a)Cyclic voltammograms were run at 50 mV per second unlessnoted otherwise. ΔE_(p) is defined as the difference between the voltagevalues at E_(a), the anodic peak current and E_(c), the cathodic peakcurrent, observed in the cyclic voltammogram. E_(1/2) represents thereversible half-wave oxidation potential and is equal to the average ofthe voltage values at E_(a), the anodic peak current and E_(c), thecathodic peak current, observed in the cyclic voltammogram. ^(b)Thesolid and open number refer to the step number on a Stouffer 21-stepsensitivity wedge. ^(c)The exposure time was 60 seconds and the heatingtime was 30 seconds. ^(d)The exposure time was 120 seconds and theheating time was 60 seconds.

The data from absorbance measurements of fresh and 60° C. aged samplesindicate that the stability of dyes in Examples 3-8 and ComparativeExamples 1-2 in the presence of TTT is dependent on the oxidationpotential of the dye; dyes are relatively unstable in the presence ofTTT if their oxidation potential is less than about 0.65 V versus SCE.In addition, the sensitivity of samples containing dyes with anoxidation potential less than about 0.65 V versus SCE decreases moreseverely when aged at 60° C.

The sensitivity results for the fresh coatings indicate than thesensitivity is dependent on the oxidation potential of the dyes. As theoxidation potential of the dye increases, the sensitivity of thecoatings tends to decrease; a dramatic decrease in sensitivity occursabove an oxidation potential of about 0.7 V versus SCE.

EXAMPLES 9-13 AND COMPARATIVE EXAMPLES 3-4

These examples demonstrate that the shelf lift and sensitivity ofcoatings containing poly(tetrahydropyranyl methacrylate),ditolyliodonium hexafluorophosphate, and squarylium dye depend on theoxidation potential of the dye.

Coating formulations consisted of 2.0 g of 9% by weightpoly(tetrahydropyranylmethacrylate) in methylethylketone, 0.03 gditolyliodonium hexafluorophosphate, and dye. The formulations werecoated with a No. 5 coating rod onto 200 micron thick grained andanodized aluminum printing plate base and dried with a heat gun.

Example 9, 0.016 g Dye 1a.

Example 10, 0.018 g Dye 1b.

Example 11, 0.015 g Dye 1c.

Example 12, 0.023 g Dye 1d.

Example 13, 0.016 g Dye 1e.

Comparative Example 3, 0.006 g Dye 1h.

Comparative Example 4, 0.009 g Dye 1i.

Absorbances at λ_(max) were determined from near infrared spectra(integrating sphere) of a sample of each of Examples 9-13 andComparative Examples 3 and 4 when fresh and after aging at 60° C. Theresults are given in Table 4.

Relative sensitivities were determined by exposing a sample of each ofExamples 9-13 and Comparative Examples 3-4 (fresh and after aging at 60°C.) for 6 minutes through a Stouffer 21-step sensitivity wedge and a #25Wratten gelatin cutoff light filter (Eastman Kodak, Rochester, N.Y.)using a Model 70 tungsten light source (3M, St. Paul, Minn). The plateswere developed using PCX positive plate developer. The plates were theninked with black newspaper ink in the presence of water. Sensitivity isproportional to the number of clean, open steps on the plate that didnot accept ink. An open step is defined as an area where all the coatingwas developed off the plate to reveal the hydrophilic aluminum surface.A solid step is defined as the first step which accepted a full densityof black ink. The results are given in Table 4.

TABLE 4 λ_(max) Example or ΔE_(p) Absorbance: Comparative E_(1/2) vs.SCE Fresh and after Relative sensitivity of fresh Example (CH₂Cl₂)^(a)aging at 60° C. plates and after aging at 60° C.^(b) λ_(max) 805 nmFresh: Open 6, Solid 9. Example 9 ΔE_(p) = 0.074 V Fresh: 809 nm (0.859)1 day, 60° C.: All the coating Dye 1a E_(1/2) = 0.51 V 1 day: 837 nm(0.553) developed off the plate. 2 days: 835 nm (0.414) 3 days: 837 nm(0.368) λ_(max) 810 nm Fresh: Open 5, Solid 7. Example 10 ΔE_(p) = 0.066V Fresh: 810 nm (0.847) 1 day, 60° C.: Open 5, Solid 9. Dye 1b E_(1/2) =0.54 V 1 day: 819 nm (0.717) 3 days, 60° C.: All the coating 2 days: 826nm (0.593) developed off the plate. 3 days: 830 nm (0.466) λ_(max) 792nm Fresh: Open 2, Steps 3-10 all Example 11 ΔE_(p) = 0.079 V Fresh: 793nm (0.841) accepted the same low density Dye 1c E_(1/2) = 0.61 V 1 day:803 nm (0.773) of ink, Solid 11. 2 days: 817 nm (0.621) 1 day, 60° C.:Open 4, Solid 8. 3 days: 814 nm (0.556) 3 days, 60° C.: All the coatingdeveloped off the plate. Example 12 ΔE_(p) = 0.089 V λ_(max) 811 nmFresh: Open 3, Solid 8, some Dye 1d E_(1/2) = 0.62 V Fresh: 813 nm(0.480) background staining. 1 day: 814 nm (0.415) 1 day, 60° C.: Open1, Steps 2- 2 days: 814 nm (0.367) 11 all accepted the same low 3 days:817 nm (0.312) density of ink, Solid 12. 3 days, 60° C.: Open 2, Solid8. λ_(max) 796 nm Fresh: Open 5, Solid 7. Example 13 ΔE_(p) = 0.077 VFresh: 795 nm (0.865) 1 days, 60° C.: Open 4, Steps 5- Dye 1e E_(1/2) =0.68 V 1 day: 799 nm (0.842) 11 all accepted the same low 2 days: 799 nm(0.835) density of ink, Solid 12. 3 days: 800 nm (0.810) 3 days, 60° C.:Open 1, Steps 2- 12 all accepted the same low density of ink, Solid 13.λ_(max) 768 nm Fresh: <1 Open step, Solid 4. Comparative ΔE_(p) = 0.077V Fresh: 768 nm (0.742) 3 days, 60° C.: <1 Open step, Example 3 E_(1/2)= 0.67 V 1 day: 768 (0.728) Solid 4. Dye 1h 2 days: 767 nm (0.720) 3days: 766 nm (0.712) λ_(max) 659 nm Fresh: Solid 13, Steps 1-12 allComparative ΔE_(p) = 0.077 V Fresh: 659 nm (0.790) accepted some ink.Example 4 E_(1/2) = 0.48 V 1 day: 660 nm (0.638) 1 days, 60° C.: Solid20, Steps Dye 1i 2 days, 661 nm (0.557) 1-19 all accepted some ink. 3days: 660 nm (0.491) 3 days, 60° C.: Solid 17, Steps 1-16 all acceptedsome ink. ^(a)Cyclic voltammograms were run at 50 mV per second unlessnoted otherwise. ΔE_(p) is defined as the difference between the voltagevalues at E_(a), the anodic peak current, and E_(c), the cathodic peakcurrent, observed in the cyclic voltammogram. E_(1/2) represents thereversible half-wave oxidation potential and is equal to the average ofthe voltage values at E_(a), the anodic peak current and E_(c), thecathodic peak current, observed in the cyclic voltammogram. ^(b)Thesolid and open number refer to the step number on a Stouffer 21-stepsensitivity wedge.

The data from absorbance measurements of fresh and 60° C. aged samplesindicate that the stability of dyes in Examples 9-13 and ComparativeExamples 3-4 in the presence of di-(4-tolyl)iodonium hexafluorophosphateis dependent on the oxidation potential of the dye; dyes are relativelyunstable in the presence of di-(4-tolyl)iodonium hexafluorophosphate iftheir oxidation potential is less than about 0.65 V versus SCE. InExamples 9-11 containing dyes with low oxidation potentials, all thecoating developed off the plate in the aged samples, indicating thermalgeneration of acid at 60° C., resulting in cleavage of the poly(tetrahydropyranyl methacrylate) to polymethacyrylic acid which issoluble in the developer.

These results suggest that the squarylium dyes disclosed in U.S. Pat.No. 5,401,607 with oxidation potentials less than about 0.5 V versus SCEwould be unstable in the presence of iodonium salts such asdi-(4-tolyl)iodonium hexafluorophosphate and therefore not be useful incoatings containing them and iodonium salts.

The results also show that coatings containing Dye 1e anddi-(4-tolyl)iodonium hexafluorophosphate are significantly moresensitive than Dye 1h and di-(4-tolyl)iodonium hexafluorophosphate. Dye1h belongs to the class of squarylium dyes disclosed in U.S. Pat. No.5,401,607, wherein it states that squarylium dyes of that class withoxidation potentials above about 0.5 V versus SCE are not useful in thepresence of iodonium salts for photogeneration of Bronsted acid.However, the dihydroperimidine dyes disclosed in this application areuseful with iodonium salts, giving adequate sensitivity for practicalapplications even though their oxidation potentials are greater than 0.5V versus SCE. Furthermore, the dihydroperimidine dyes are even moreuseful with iodonium salts since they can achieve good sensitivity andstability at oxidation potentials well above 0.5 V versus SCE.

EXAMPLE 14

A solution consisting of 4 g of 10% by weight poly(tetrahydropyranylmethacrylate) in 2:1 methylethylketone and Dowanol PM(Dow Chemical Co., Midland, Mich.), 0.030 g Dye 1e, and 0.060 gdi-(4-tolyl)iodonium hexafluorophosphate was coated with a No. 5 coatingrod onto 150 micron thick grained and anodized aluminum printing platebase that had been surface treated with polyacrylic acid and dried for 2minutes at 80° C. The absorption spectrum of the coating was obtainedfor a fresh sample and the same sample after accelerated aging at 60° C.for 1,2, and 3 days. The aged sample was tested for loss of absorbanceby Dye 1e at 830 nm. (See Table 5).

Six 4″×6″ (10.2 cm×15.2 cm) samples of the coating, 14A-14F, wereprepared for accelerated aging tests at 60° C. for 1,2, and 3 days.Unexposed, aged plate samples 14A, 14B, and 14C were tested for weightloss after development with a developer consisting of the ratio 3.41 gtriethanolamine, 1.59 g concentrated HCl, and 95 g water. (See Table 6).

Aged plate samples 14D, 14E, and 14F were scanned with the laser diodeexposure assembly. The sample was weighed before exposure, afterexposure, after hand development with a developer consisting of theratio 3.41 g triethanolamine, 1.59 g concentrated HCl, and 95 g water,and after hand washing with acetone to remove any remaining coating.From these weighings, the coating weight (g/m²), % mass lost afterexposure, % mass lost after development, and % mass lost after acetonerinse were determined. The results are summarized in Table 7.

EXAMPLE 15

A solution consisting of 4 g of 10% poly (tetrahydropyranylmethacrylate)in 2:1 methylethylketone and Dowanol PM, 0.030 g Dye 1a, and 0.060 gdi-(4-tolyl) iodonium hexafluorophosphate was coated with a No. 5coating rod onto 150 micron thick grained and anodized aluminum printingplate base that had been surface treated with polyacrylic acid and driedfor 2 minutes at 80° C. The absorption spectrum of the coating wasobtained for a fresh sample and the same sample after accelerated agingat 60° C. for 1,2, and 3 days. The aged sample was tested for loss ofabsorbance by Dye 1e at 830 nm. (See Table 5).

Six 4″×6″ (10.2 cm×15.2 cm) samples, 15A-15F, were prepared foraccelerated aging at 60° C. for 1,2, and 3 days. Unexposed, aged platesamples 15A, 15B, and 15C were tested for weight loss after developmentwith a developer consisting of the ratio 3.41 g triethanolamine, 1.59 gconcentrated HCl, and 95 g water. (See Table 6).

Aged plate samples 15D, 15E, and 15F were scanned with the laser diodeexposure assembly. The sample was weighed before exposure, afterexposure, after hand development with a developer consisting of theratio 3.41 g triethanolamine, 1.59 g concentrated HCl, and 95 g water,and after hand washing with acetone to remove any remaining coating.From these weighings, the coating weight (g/m²), % mass lost afterexposure, % mass lost after development, and % mass lost after acetonerinse are determined. The results are summarized in Table 7.

TABLE 5 Loss of absorbance after accelerated aging. Abs. Abs. Abs. Abs.(830 nm) (830 nm) (830 nm) (830 nm) of fresh after 1 day after 2 daysafter 3 days Sample sample at 60° C. at 60° C. at 60° C. Example 140.781 0.763 0.773 0.722 Example 15 0.891 0.616 0.471 0.408

TABLE 6 Weight loss of unexposed and developed samples after acceleratedaging Coating wt % Weight lost after development Sample (g/m²) 1 day,60° C. 2 day, 60° C. 3 day, 60° C. Ex. 14A 1.02  3.2% — — Ex. 14B 0.93 — 3.5% — Ex. 14C 0.82 — —  5.5% Ex. 15A 0.76 19.5% — — Ex. 15B 0.90 —88.5% — Ex. 15C 1.00 — — 98.7%

TABLE 7 Weight loss of exposed and developed samples after acceleratedaging. % Wt loss after % Wt loss after Coat. % Wt. loss after exposuredevelopment acetone wash wt. 1 day, 2 day, 3 day, 1 day, 2 day, 3 day, 1day, 2 day, 3 day, Sample (g/m²) 60° C.^(a) 60° C.^(b) 60° C.^(b) 60°C.^(a) 60° C.^(b) 60° C.^(b) 60° C.^(a) 60° C.^(b) 60° C.^(b) Ex. 14D0.96 19.6 — — 80.4 — — 0 — — Ex. 14E 0.91 — 17 — — 81.6 — — 1.4 — Ex.14F 0.96 — — 21.6 — — 77   — — 1.4 Ex. 15D 0.90 15.7 — — 84.3 — — 0 — —Ex. 15E 0.87 — 17 — — 83   — — 0   — Ex. 15F 0.94 — — 20.7 — — 78.6 — —0.7 ^(a)Exposed at 6 rev/sec. ^(b)Exposed at 8 rev/sec.

The results of Examples 14 and 15 show that Dye 1e is a much more stabledye than Dye 1a when used with di-(4-tolyl)iodonium hexafluorophosphate.Table 4 indicates that the absorption of Dye 1a decreases 54% after 3days at 60° C., whereas the absorption of Dye 1e decreases only 7.5%after 3 days at 60° C. Table 5 indicates that 98.7% of the coatingdeveloped off an unexposed sample containing Dye 1a after 3 days at 60°C., whereas only 5.5% of the coating developed off an unexposed samplecontaining Dye 1e after 3 days at 60° C. The instability of Dye 1a maybe due to oxidation of Dye 1a (E_(1/2)=0.51 V versus SCE) bydi-(4-tolyl)iodonium hexafluorophosphate (peak reduction potential ofapproximately—0.67 V versus SCE) to generate acid, which cleavespoly(tetrahydropyranylmethacrylate) to poly (methacrylic acid), which iseasily developed off the plate with the developer of Example 15. Platescontaining Dye 1e would be expected to have good shelf-stability whereasplates containing Dye 1a would not.

COMPARATIVE EXAMPLE 5

Example 15 was repeated without di-(4-tolyl)iodonium hexafluorophosphateto give a coating weight of 0.76 g/m². A 4″×6″ (10.2 cm×15.2 cm) samplewas scanned at 6 rev/sec to give a 43.2% weight loss after imaging.Hand-development with the same developer used in Example 15 resulted ina further 30.5% weight loss. A final acetone washing removed a residual26.3% of the coating.

EXAMPLE 16

A solution consisting of 2 g of 25% by weight poly(tetrahydropyranylmethacrylate) in Dowanol PM (primarily1-methoxy-2-propanol, Dow Chemical Co., Midland, Mich.), 0.016 g Dye 1e,0.04 g 2-methoxy-4-aminophenyl diazonium hexafluorophosphate, and 1.22 gmethylethylketone was coated with a No. 5 coating rod onto 200 micronthick grained and anodized aluminum printing plate base, and dried fortwo minutes at 80° C. Separate areas of the plate were scanned with thelaser diode exposure assembly at a rate of 4, 6, 8, 10 and 12revolutions per second (339, 508, 678, 848, and 1,018 centimeters persecond, respectively). The plate was developed using PCX positive platedeveloper. The plates were then inked with black newspaper ink in thepresence of water. The areas exposed at 4,6, and 8 revolutions persecond remained free of ink. The area exposed at 10 revolutions persecond had slight toning of ink. The area exposed at 12 revolutions persecond had severe toning of ink.

EXAMPLE 17

A solution consisting of 4.0 g of 10% by weight poly(tetrahydropyranylmethacrylate) in methylethylketone, 0.034 g Dye 1e,and 0.060 g of (η⁶-xylenes) (η⁵-cyclopentadienyl)iron (II)hexafluoroantimonate was coated with a No. 5 coating rod onto 150 micronthick grained and anodized aluminum printing plate base, and dried fortwo minutes at 8° C. A 4″×6″ (10.2 cm×15.2 cm) sample of the coatedplate was scanned with the laser diode exposure assembly at 6revolutions per second (508 centimeters per second). The coating weightloss after exposure was 48%. The exposed sample was then hand-developedwith PCX positive plate developer as in Example 1, resulting in afurther coating weight loss of 49%, and leaving a residual coatingweight of 1%. The residual material was detected after further washingwith acetone.

EXAMPLE 18

A solution consisting of 2.0 g of 10% by weight poly(tetrahydropyranylmethacrylate) in methylethylketone, 0.016 g Dye 1e,0.030 mg (η⁶-xylenes) (η⁵-cyclopentadienyl) iron (II)hexafluoroantimonate, and 0.012 mg diamyl oxalate was coated with a No.5 coating rod onto 150 micron thick grained and anodized aluminumprinting plate base, and dried for two minutes at 80° C. The sample wasirradiated and developed as in Example 16. The sample lost 44% of itsweight after irradiation, and the other 56% of its weight afterdevelopment.

EXAMPLE 19

A solution consisting of 2.0 g of 10% by weight Novolak SD-126A inmethylethylketone, 0.020 g di-(4-tolyl) iodonium hexafluorophosphate,0.080 g Dissolution inhibitor 1, and 0.016 g Dye 1e was coated using aNo. 5 coating rod onto 200 micron thick grained and anodized aluminumprinting plate base and dried for two minutes at 80° C. The plate wasirradiated using the laser diode exposure assembly at 3, 6, 7, 8, 9, and11 revolutions per second. The plate was developed by wiping it with 8%by weight aqueous sodium metasilicate solution. Irradiated areas washedaway to give a clear image at up to 8 revolutions per second.

EXAMPLE 20

A solution consisting of 4.0 g of 15% by weight Novolak SD-126A inmethylethylketone, 0.060 g di-(4-tolyl) iodonium hexafluorophosphate,0.120 g Dissolution inhibitor 1, 0.017 g of Dye 1e and 0.004 g ForonBrilliant Blue (Sandoz Chemicals Corp., Charlotte, N.C.) dye was coatedwith a No. 16 coating rod on top of the copper layer in a film composedof a 4 micron copper layer on 50 micron thick Kapton polyimide substrate(E. I. DuPont de Nemours, Wilmington, Del.) and dried for two minutes at80° C. The film was imaged using the laser diode exposure assembly at adrum speed of 4 revolutions per second. The image was developed bysoaking the film in 6% by weight aqueous sodium metasilicate solutionfor 30 seconds, then rinsed with tap water. Copper was etched from theKapton in the irradiated areas using a bath consisting of 150 g EnplateAD-4851 (Asarco Inc./Ethone-OMI, Inc., New Haven, Conn.) per liter of 2%sulfuric acid.

EXAMPLE 21

Magenta pigment construction: A coating solution was prepared consistingof 2.5 g of 20 weight % poly (tetrahydropyranylmethacrylate) in DowanolPM, 0.08 g ditolyliodonium hexafluorophosphate, 0.04 g Dye 1e, 0.08 gmagenta pigment millbase, and 1.5 g methylethylketone. The magentamillbase contained 0.0967 g RS magenta pigment dispersion (RBHDispersants, Inc., subsidiary of Reichold Chemicals, Bound Brook, N.J.),0.0967 g Joncryl 690 (acrylic resin, S. C. Johnson and Son, Racine,Wis.), 0.0116 g Disperbyk 161 (BYK Chemie, Wallingford, Conn.), 0.1987 gmethylethylketone, and 0.5961 g Dowanol PM. The coating solution wasprepared by addition of Dye 1e to methylethylketone followed by theaddition of the iodonium salt, poly(tetrahydropyranylmethacrylate)solution, and magenta pigment millbase in that order. This solution wascoated onto the surface of a polyvinylalcohol release layer on 50 micronthick polyester using a No. 6 coating rod and oven dried for 2 minutesat 80° C.

Adhesive receptor sheet: A solution consisting of 1.5 g Pliolyte SSA(styrene-butadiene copolymer, Goodyear Tire and Rubber Co., Akron,Ohio), 1.0 g Pliolyte AC (styrene-acrylate copolymer, Goodyear Tire andRubber Co., Akron, Ohio), and 7.5 g toluene was coated with a No. 4coating rod onto Matchprint commercial proofing paper stock (3M, St.Paul, Minn.).

The magenta pigment construction was laminated to the adhesive receptorsheet and the polyvinylalcohol-polyester release liner peeled away. Theresulting magenta pigmented proofing film was imaged using the laserdiode exposure assembly at a drum speed of 6 revolutions per second to amagenta color separation digital image. The exposed film was developedwith Matchprint III developer (3M, St. Paul, Minn.). The exposed areasof the film developed off the film to give a positive magenta colorseparation proof.

What is claimed is:
 1. An acid-generating composition comprising: (a) aphotochemical acid progenitor; and (b) a squarylium dye having a nucleusof the general formula:

wherein: R¹ to R⁴ are groups independently selected from hydrogen,alkyl, cycloalkyl, aralkyl, carboalkoxyalkyl and carboaryloxyalkylgroups; X represents>CR⁵R⁶, >POR⁷, or >BOR⁷ wherein: R⁵ and R⁶ areindependently selected from hydrogen, alkyl, cycloalkyl, alkyl, andaralkyl groups; or R¹ and R⁵, and/or R² and R⁶, and/or R³ and R⁵, and/orR⁴ and R⁶, and/or R⁵ and R⁶ represent the necessary atoms to complete a5-, 6- or 7-membered ring; and R⁷ represents an alkyl group.
 2. Thecomposition of claim 1 wherein R¹ to R⁴ are independently selected fromhydrogen; a substituted or unsubstituted alkyl or cycloalkyl grouphaving from 1 to 20 carbon atoms; an aralkyl group having from 6 to 20carbon atoms; a carboalkoxyalkyl group with the alkoxy group having from1 to 20 carbon atoms; and a carboaryloxyalkyl group with the aryloxygroup having from 5 to 20 carbon atoms.
 3. The composition of claim 1wherein R⁵ and R⁶ are independently selected from hydrogen; an alkyl orcycloalkyl group having from 1 to 20 carbon atoms; and a substituted orunsubstituted aryl group having from 5 to 20 carbon atoms.
 4. Thecomposition of claim 3 wherein R⁵ and R⁶ are independently selected fromthe group consisting of: —CH₂OH, —CH₂OR⁸, —CH₂OCH₂CO₂R⁸, —CH₂OC (═O)R⁸,—CH₂OSO₂R⁹, and —CH₂OSi(R⁹)₃, wherein R⁸ is independently an alkyl,alkaryl, aralkyl or aryl group and R⁹ is an alkyl or alkaryl group. 5.The composition of claim 4 wherein R⁸ is independently an alkyl,alkaryl, aralkyl or aryl group having from 1 to 20 carbon atoms and R⁹is an alkyl or alkaryl group having from 1 to 20 carbon atoms.
 6. Thecomposition of claim 1 wherein R⁷ is an alkyl group having from 1 to 20carbon atoms.
 7. The composition of claim 1 wherein R¹ and R⁵ are takentogether and R³ and R⁵ are taken together to form lactam groups.
 8. Thecomposition of claim 1 wherein said acid progenitor is selected from thegroup consisting of trihalomethyl-substituted s-triazines, onium salts,iron arene complexes, nitrobenzyl esters, and sulfonic acid esters. 9.The composition of claim 8 wherein said trihalomethyl-substituteds-triazine is selected from the group consisting of2,4,6-tris(trichloromethyl)-s-triazine;2-(4-methoxyphenyl)-4,6-bis-(trichloromethyl)-s-triazine; and2-(4-methoxy-1-naphthalenyl)-4,6-bis(trichloromethyl)-s-triazine. 10.The composition of claim 8 wherein said onium salt is selected from thegroup consisting of diaryliodonium salts, triarylsulfonium salts,triarylselenonium salts, dialkylphenacylsulfonium salts,dialkyl-4-hydroxyphenylsulfonium salts, and aryldiazonium salts.
 11. Thecomposition of claim 10 wherein the onium salt comprisesdi(4-tolyl)iodonium hexafluorophosphate or 2-methoxy-4-aminophenyldiazonium hexafluorophosphate.
 12. The composition of claim 8 whereinsaid iron arene complex comprises (η⁶-isopropylbenzene)(η⁵-cyclopentadienyl)iron (II) hexafluorophosphate or (η⁶-Xylenes)(η⁵-cyclopentadienyl)iron (II) hexafluoroantimonate.
 13. The compositionof claim 1 further comprising a polymeric binder.
 14. The composition ofclaim 13 wherein said polymeric binder is selected from the groupconsisting of novolak resins, melamine folmaldehyde resins, andtetrahydropyranyl(meth)acrylate homo- and co-polymers.
 15. Thecomposition of claim 13 wherein the amount of squarylium dye present isfrom 0.01 to 0.6 parts by weight relative to one part by weight of saidacid progenitor.
 16. The composition of claim 13 wherein the amount ofsaid binder present is from 2 to 100 parts by weight relative to onepart by weight of said acid progenitor.
 17. The composition of claim 13wherein the amount of said binder present is from 5 to 50 parts byweight relative to one part by weight of said acid progenitor.
 18. Thecomposition of claim 13 further comprising a crosslinking agent or adissolution inhibitor.
 19. The composition of claim 18 wherein thecrosslinking agent comprises a compound having two or more alkoxymethylgroups, methylol groups, or acetoxymethyl groups.
 20. The composition ofclaim 18 wherein the amount of crosslinking agent present is from 0.1 to100 parts by weight relative to one part by weight of the acidprogenitor.
 21. The composition of claim 18 wherein the amount ofcrosslinking agent present is from 0.2 to 50 parts by weight relative toone part by weight of the acid progenitor.
 22. An imaging compositioncomprising a substrate having coated thereon a photosensitive layercomprising: (a) a photochemical acid progenitor; and (b) a squaryliumdye having a nucleus of the general formula:

wherein: R¹ to R⁴ are independently selected from hydrogen, alkyl,cycloalkyl, aralkyl, carboalkoxyalkyl and carboaryloxyalkyl groups; Xrepresents >CR⁵R⁶, >POR⁷, or >BOR⁷ wherein: R⁵ and R⁶ are independentlyselected from hydrogen, alkyl, cycloalkyl, aryl, and aralkyl groups; orR¹ and R⁵, and/or R² and R⁶, and/or R³ and R⁵, and/or R⁴ and R⁶, and/orR⁵ and R⁶ represent the necessary atoms to complete a 5-, 6- or7-membered ring; and R⁷ represents an alkyl group.
 23. The compositionof claim 22 wherein said photosensitive layer further comprises abinder.
 24. The composition of claim 22 wherein said substrate isselected from the group consisting of grained and anodized aluminumprinting plate base, copper plated polyimide, and polyester.